High-level exogenous glutamic acid-independent production of poly-(γ-glutamic acid) with organic acid addition in a new isolated Bacillus subtilis C10

2012 ◽  
Vol 116 ◽  
pp. 241-246 ◽  
Author(s):  
Huili Zhang ◽  
Jianzhong Zhu ◽  
Xiangcheng Zhu ◽  
Jin Cai ◽  
Anyi Zhang ◽  
...  
Author(s):  
Sulhattin YASAR ◽  
Ramazan TOSUN

In order to enrich soybean meal (SBM) by microbial fermentation, SBM (3 mm particle size) with 78 or 85% moisture content were inoculated with 0.0 or 1x107 CFU/g (colony forming unit) Bacillus subtilis ATCC PTA-6737 and fermented at 37 oC for 0, 24, 48 and 72 h. There was a marked decrease in pH with 85% moisture content, associated at higher organic acid production, compared to increased pH at 24 h with 78% moisture content and a gradual decrease hereafter. Bacterial growth peaked at 48 h with both moisture contents. Fermenting SBM increased crude ash level by 65%, soluble amino acid nitrogen by 2.7 folds and degraded phytic acid by 65-75%. Moreover, there was a high level of organic acid production despite of decreased crude protein by 6-7%, but the effect of high moisture level was more pronounced in all case. In conclusion, fermentation SBM with water content of 85% at 35 oC by B. subtilis provided SBM an appreciable amount of bio-functionalities such reduced phytate content, increased soluble amino acid content and more importantly fortified with organic acids. The fermented SBM can therefore be used an antimicrobial agent due to its high organic acid level in animal nutrition.


1951 ◽  
Vol 191 (1) ◽  
pp. 305-307
Author(s):  
Lloyd T. Jenkins ◽  
Leon S. Ciereszko

Nature ◽  
1960 ◽  
Vol 186 (4727) ◽  
pp. 818-818
Author(s):  
HARUO MOMOSE ◽  
YÔNOSUKE IKEDA

AMB Express ◽  
2013 ◽  
Vol 3 (1) ◽  
pp. 36 ◽  
Author(s):  
Aditya R Bhat ◽  
Victor U Irorere ◽  
Terry Bartlett ◽  
David Hill ◽  
Gopal Kedia ◽  
...  

1996 ◽  
Vol 82 (1) ◽  
pp. 84-87 ◽  
Author(s):  
Haruhiko Yokoi ◽  
Tomomi Arima ◽  
Jun Hirose ◽  
Sachio Hayashi ◽  
Yoshiyuki Takasaki

2002 ◽  
Vol 184 (7) ◽  
pp. 1998-2004 ◽  
Author(s):  
Takako Murakami ◽  
Koki Haga ◽  
Michio Takeuchi ◽  
Tsutomu Sato

ABSTRACT The Bacillus subtilis spoIIIJ gene, which has been proven to be vegetatively expressed, has also been implicated as a sporulation gene. Recent genome sequencing information in many organisms reveals that spoIIIJ and its paralogous gene, yqjG, are conserved from prokaryotes to humans. A homologue of SpoIIIJ/YqjG, the Escherichia coli YidC is involved in the insertion of membrane proteins into the lipid bilayer. On the basis of this similarity, it was proposed that the two homologues act as translocase for the membrane proteins. We studied the requirements for spoIIIJ and yqjG during vegetative growth and sporulation. In rich media, the growth of spoIIIJ and yqjG single mutants were the same as that of the wild type, whereas spoIIIJ yqjG double inactivation was lethal, indicating that together these B. subtilis translocase homologues play an important role in maintaining the viability of the cell. This result also suggests that SpoIIIJ and YqjG probably control significantly overlapping functions during vegetative growth. spoIIIJ mutations have already been established to block sporulation at stage III. In contrast, disruption of yqjG did not interfere with sporulation. We further show that high level expression of spoIIIJ during vegetative phase is dispensable for spore formation, but the sporulation-specific expression of spoIIIJ is necessary for efficient sporulation even at the basal level. Using green fluorescent protein reporter to monitor SpoIIIJ and YqjG localization, we found that the proteins localize at the cell membrane in vegetative cells and at the polar and engulfment septa in sporulating cells. This localization of SpoIIIJ at the sporulation-specific septa may be important for the role of spoIIIJ during sporulation.


2006 ◽  
Vol 188 (4) ◽  
pp. 1411-1418 ◽  
Author(s):  
Guangnan Chen ◽  
Amrita Kumar ◽  
Travis H. Wyman ◽  
Charles P. Moran

ABSTRACT At the onset of endospore formation in Bacillus subtilis the DNA-binding protein Spo0A directly activates transcription from promoters of about 40 genes. One of these promoters, Pskf, controls expression of an operon encoding a killing factor that acts on sibling cells. AbrB-mediated repression of Pskf provides one level of security ensuring that this promoter is not activated prematurely. However, Spo0A also appears to activate the promoter directly, since Spo0A is required for Pskf activity in a ΔabrB strain. Here we investigate the mechanism of Pskf activation. DNase I footprinting was used to determine the locations at which Spo0A bound to the promoter, and mutations in these sites were found to significantly reduce promoter activity. The sequence near the −10 region of the promoter was found to be similar to those of extended −10 region promoters, which contain a TRTGn motif. Mutational analysis showed that this extended −10 region, as well as other base pairs in the −10 region, is required for Spo0A-dependent activation of the promoter. We found that a substitution of the consensus base pair for the nonconsensus base pair at position −9 of Pskf produced a promoter that was active constitutively in both ΔabrB and Δspo0A ΔabrB strains. Therefore, the base pair at position −9 of Pskf makes its activity dependent on Spo0A binding, and the extended −10 region motif of the promoter contributes to its high level of activity.


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